KCF-S cluster No. 672 (13 metabolites)

Corresponding Phytochemical cluster No. 4


Plant Species


Cumulative plant class count

class name count
asterids 46

Cumulative family count

class name count
Loganiaceae 46

KEGG BRITE br08003 External link 512


Categories (1)

br08003 Category # of metabolite
Indole alkaloids 2

metabolites link (3)

br08003 Category KEGG ID KNApSAcK ID
Indole alkaloids C09084 C00001695
Indole alkaloids C06522 C00001770
Indole alkaloids C06522 C00025213

Metabolite list (13)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
figure
C00001695 External link 512 Brucine
CHEMBL501756
CHEMBL1333042
CHEMBL1515857
CHEMBL1573549
CHEMBL2361237
C083806
11 / 24 / 21 11 / 8
C00001770 External link 512 Strychnine
CHEMBL33495
CHEMBL227934
CHEMBL1436908
CHEMBL1446958
CHEMBL1609139
D013331
102 / 46 / 46 5 / 5
C00025153 External link 512 alpha-Colubrine
CHEMBL2164940
C00025155 External link 512 beta-Colubrine
CHEMBL1994566
C00025156 External link 512 Brucine N-oxide
CHEMBL343357
C083067
5 / 3 / 0 5 / 0
C00025165 External link 512 Diaboline
CHEMBL1969794
C00025199 External link 512 Pseudobrucine
/ 16-Hydroxybrucine
CHEMBL2004313
CHEMBL2164941
C00025200 External link 512 Pseudostrychnine
CHEMBL1970129
CHEMBL2164943
C00025213 External link 512 Certox
/ Strychnine
/ (-)-Strychnine
CHEMBL33495
CHEMBL227934
CHEMBL1436908
CHEMBL1446958
CHEMBL1609139
D013331
102 / 46 / 46 5 / 5
C00027669 External link 512 12-Hydroxy-11-methoxydiaboline
C00029380 External link 512 11-Methoxydiaboline
C00037174 External link 512 Genostrychnine
CHEMBL138585
C083068
4 / 3 / 0
C00037693 External link 512 Protostrychnine

Human Protein / Gene in interactions

105 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P20309 Muscarinic acetylcholine receptor M3 Acetylcholine receptor C00001695 C00001770 C00025156 C00025213 C00037174 1 / 0
P08172 Muscarinic acetylcholine receptor M2 Acetylcholine receptor C00001695 C00001770 C00025156 C00025213 C00037174 2 / 0
P11229 Muscarinic acetylcholine receptor M1 Acetylcholine receptor C00001695 C00001770 C00025156 C00025213 C00037174 0 / 0
P08173 Muscarinic acetylcholine receptor M4 Acetylcholine receptor C00001695 C00001770 C00025156 C00025213 C00037174 0 / 0
P08912 Muscarinic acetylcholine receptor M5 Acetylcholine receptor C00001695 C00001770 C00025156 C00025213 0 / 0
O00255 Menin Unclassified protein C00001695 C00001770 C00025213 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001695 C00001770 C00025213 1 / 2
O75496 Geminin Unclassified protein C00001695 C00001770 C00025213 0 / 0
P03372 Estrogen receptor NR3A1 C00001770 C00025213 1 / 1
P29466 Caspase-1 C14 C00001770 C00025213 0 / 0
P17252 Protein kinase C alpha type Alpha C00001770 C00025213 0 / 0
P27361 Mitogen-activated protein kinase 3 Erk C00001770 C00025213 0 / 0
P14780 Matrix metalloproteinase-9 M10A C00001770 C00025213 2 / 2
Q99250 Sodium channel protein type 2 subunit alpha SCN alpha, NaV1.x C00001770 C00025213 2 / 2
P23415 Glycine receptor subunit alpha-1 GLR alpha C00001770 C00025213 1 / 1
P00918 Carbonic anhydrase 2 Lyase C00001770 C00025213 1 / 2
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00001770 C00025213 0 / 1
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00001770 C00025213 1 / 1
P25021 Histamine H2 receptor Histamine receptor C00001770 C00025213 0 / 0
P35367 Histamine H1 receptor Histamine receptor C00001770 C00025213 0 / 0
Q01959 Sodium-dependent dopamine transporter Dopamine C00001770 C00025213 1 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001770 C00025213 1 / 0
P18825 Alpha-2C adrenergic receptor Adrenergic receptor C00001770 C00025213 0 / 0
P13945 Beta-3 adrenergic receptor Adrenergic receptor C00001770 C00025213 0 / 0
P25024 C-X-C chemokine receptor type 1 CXC chemokine receptor C00001770 C00025213 0 / 0
P06241 Tyrosine-protein kinase Fyn Src C00001770 C00025213 0 / 0
Q08209 Serine/threonine-protein phosphatase 2B catalytic subunit alpha isoform Ser_Thr C00001770 C00025213 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001770 C00025213 0 / 1
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00001770 C00025213 1 / 8
P14416 D(2) dopamine receptor Dopamine receptor C00001770 C00025213 2 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00001770 C00025213 0 / 0
P37288 Vasopressin V1a receptor Vasopressin and oxytocin receptor C00001770 C00025213 0 / 0
P41145 Kappa-type opioid receptor Opioid receptor C00001770 C00025213 0 / 0
Q9Y271 Cysteinyl leukotriene receptor 1 Leukotriene receptor C00001770 C00025213 0 / 0
P29274 Adenosine receptor A2a Adenosine receptor C00001770 C00025213 0 / 0
P25929 Neuropeptide Y receptor type 1 Neuropeptide Y receptor C00001770 C00025213 0 / 0
P50052 Type-2 angiotensin II receptor Angiotensin receptor C00001770 C00025213 1 / 1
P17948 Vascular endothelial growth factor receptor 1 Vegfr C00001770 C00025213 0 / 0
P41968 Melanocortin receptor 3 Melanocortin receptor C00001770 C00025213 1 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00001770 C00025213 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00001770 C00025213 0 / 0
Q16539 Mitogen-activated protein kinase 14 p38 C00001770 C00025213 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00001770 C00025213 0 / 0
P08913 Alpha-2A adrenergic receptor Adrenergic receptor C00001770 C00025213 0 / 0
P21917 D(4) dopamine receptor Dopamine receptor C00001770 C00025213 0 / 0
P30988 Calcitonin receptor Calcitonin receptor C00001770 C00025213 0 / 0
P35462 D(3) dopamine receptor Dopamine receptor C00001770 C00025213 1 / 0
P41143 Delta-type opioid receptor Opioid receptor C00001770 C00025213 0 / 0
Q92731 Estrogen receptor beta NR3A2 C00001770 C00025213 0 / 1
P41595 5-hydroxytryptamine receptor 2B Serotonin receptor C00001770 C00025213 0 / 0
P25101 Endothelin-1 receptor Endothelin receptor C00001770 C00025213 0 / 0
P30411 B2 bradykinin receptor Bradykinin receptor C00001770 C00025213 0 / 0
P32245 Melanocortin receptor 4 Melanocortin receptor C00001770 C00025213 1 / 0
P32238 Cholecystokinin receptor type A Cholecystokinin receptor C00001770 C00025213 0 / 0
P08311 Cathepsin G S1A C00001770 C00025213 0 / 0
Q99720 Sigma non-opioid intracellular receptor 1 Membrane receptor C00001770 C00025213 1 / 0
P03956 Interstitial collagenase M10A C00001770 C00025213 0 / 1
P32241 Vasoactive intestinal polypeptide receptor 1 Vasoactive intestinal peptide receptor C00001770 C00025213 0 / 0
P04150 Glucocorticoid receptor NR3C1 C00001770 C00025213 0 / 1
P33765 Adenosine receptor A3 Adenosine receptor C00001770 C00025213 0 / 0
P08246 Neutrophil elastase S1A C00001770 C00025213 2 / 1
P21554 Cannabinoid receptor 1 Cannabinoid receptor C00001770 C00025213 0 / 0
P31645 Sodium-dependent serotonin transporter Serotonin C00001770 C00025213 2 / 0
P04626 Receptor tyrosine-protein kinase erbB-2 TK tyrosine-protein kinase EGFR subfamily C00001770 C00025213 5 / 9
Q12809 Potassium voltage-gated channel subfamily H member 2 KCNH, Kv10-12.x (Ether-a-go-go) C00001770 C00025213 2 / 2
P21452 Substance-K receptor Neurokinin receptor C00001770 C00025213 0 / 0
P51679 C-C chemokine receptor type 4 CC chemokine receptor C00001770 C00025213 0 / 0
P51681 C-C chemokine receptor type 5 CC chemokine receptor C00001770 C00025213 3 / 0
P50406 5-hydroxytryptamine receptor 6 Serotonin receptor C00001770 C00025213 0 / 0
P41597 C-C chemokine receptor type 2 CC chemokine receptor C00001770 C00025213 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00001770 C00025213 0 / 0
P08575 Receptor-type tyrosine-protein phosphatase C Enzyme C00001770 C00025213 2 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001770 C00025213 0 / 0
Q9NY46 Sodium channel protein type 3 subunit alpha SCN alpha, NaV1.x C00001770 C00025213 0 / 0
O76074 cGMP-specific 3',5'-cyclic phosphodiesterase PDE_5A C00001770 C00025213 0 / 0
P49146 Neuropeptide Y receptor type 2 Neuropeptide Y receptor C00001770 C00025213 0 / 0
P08588 Beta-1 adrenergic receptor Adrenergic receptor C00001770 C00025213 1 / 0
P22303 Acetylcholinesterase Hydrolase C00001770 C00025213 1 / 0
P24046 Gamma-aminobutyric acid receptor subunit rho-1 GABA-A rho C00001770 C00025213 0 / 0
P28335 5-hydroxytryptamine receptor 2C Serotonin receptor C00001770 C00025213 0 / 0
P35372 Mu-type opioid receptor Opioid receptor C00001770 C00025213 0 / 0
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00001770 C00025213 0 / 3
P25103 Substance-P receptor Neurokinin receptor C00001770 C00025213 0 / 0
P25105 Platelet-activating factor receptor PAF receptor C00001770 C00025213 0 / 0
P33032 Melanocortin receptor 5 Melanocortin receptor C00001770 C00025213 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001770 C00025213 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001770 C00025213 0 / 1
P05181 Cytochrome P450 2E1 Cytochrome P450 2E1 C00001770 C00025213 0 / 0
P23975 Sodium-dependent noradrenaline transporter Norepinephrine C00001770 C00025213 1 / 1
P25100 Alpha-1D adrenergic receptor Adrenergic receptor C00001770 C00025213 0 / 0
P30542 Adenosine receptor A1 Adenosine receptor C00001770 C00025213 0 / 0
P18089 Alpha-2B adrenergic receptor Adrenergic receptor C00001770 C00025213 0 / 0
P24557 Thromboxane-A synthase Cytochrome P450 5A1 C00001770 C00025213 1 / 1
P06239 Tyrosine-protein kinase Lck Src C00001770 C00025213 0 / 1
P25025 C-X-C chemokine receptor type 2 CXC chemokine receptor C00001770 C00025213 0 / 0
P21728 D(1A) dopamine receptor Dopamine receptor C00001770 C00025213 0 / 0
P35498 Sodium channel protein type 1 subunit alpha SCN alpha, NaV1.x C00001770 C00025213 3 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00001770 C00025213 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00001770 C00025213 1 / 4
A8MPY1 Gamma-aminobutyric acid receptor subunit rho-3 GABA-A rho C00001770 C00025213 0 / 0
P28476 Gamma-aminobutyric acid receptor subunit rho-2 GABA-A rho C00001770 C00025213 0 / 0
P28223 5-hydroxytryptamine receptor 2A Serotonin receptor C00001770 C00025213 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001695 3 / 3
P02545 Prelamin-A/C Unclassified protein C00001695 11 / 10
Q16637 Survival motor neuron protein Unclassified protein C00001695 4 / 1

13 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
1131 CHRM3, EGBRS, HM3 cholinergic receptor, muscarinic 3 C00001695 C00001770 C00025156 C00025213
1129 CHRM2, HM2 cholinergic receptor, muscarinic 2 C00001695 C00001770 C00025156 C00025213
1132 CHRM4, HM4, M4R cholinergic receptor, muscarinic 4 C00001695 C00001770 C00025156 C00025213
2741 GLRA1, HKPX1, STHE glycine receptor, alpha 1 C00001695 C00001770 C00025213
1128 CHRM1, HM1, M1, M1R cholinergic receptor, muscarinic 1 C00001695 C00025156
6331 SCN5A, CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD, HH1, ICCD, IVF, LQT3, Nav1.5, PFHB1, SSS1, VF1 sodium channel, voltage-gated, type V, alpha subunit C00001770 C00025213
581 BAX, BCL2L4 BCL2-associated X protein C00001695
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00001695
842 CASP9, APAF-3, APAF3, ICE-LAP6, MCH6, PPP1R56 caspase 9, apoptosis-related cysteine peptidase (EC:3.4.22.62) C00001695
1133 CHRM5, HM5 cholinergic receptor, muscarinic 5 C00025156
5743 PTGS2, COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2, hCox-2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase) (EC:1.14.99.1) C00001695
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00001695
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00001695

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (64)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#100100 Abdominal muscles, absence of, with urinary tract abnormality and cryptorchidism P20309
#103780 Alcohol dependence P08172
P14416
P31645
#614373 Amyotrophic lateral sclerosis 16, juvenile; als16 Q99720
#602025 Body mass index quantitative trait locus 9; bmiq9 P41968
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#162800 Cyclic neutropenia P08246
#612522 Diabetes mellitus, insulin-dependent, 22; iddm22 P51681
#607208 Dravet syndrome P35498
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#613721 Epileptic encephalopathy, early infantile, 11; eiee11 Q99250
#615363 Estrogen resistance; estrr P03372
#613659 Gastric cancer P04626
#137215 Gastric cancer, hereditary diffuse; hdgc P04626
#604403 Generalized epilepsy with febrile seizures plus, type 2; gefsp2 P35498
#231095 Ghosal hematodiaphyseal dysplasia; ghdd P24557
#137800 Glioma susceptibility 1; glm1 P04626
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#609423 Human immunodeficiency virus type 1, susceptibility to P41597
P51681
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#149400 Hyperekplexia, hereditary 1; hkpx1 P23415
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603932 Intervertebral disc disease; idd P14780
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#613688 Long qt syndrome 2; lqt2 Q12809
#211980 Lung cancer P00533
P04626
#608516 Major depressive disorder; mdd P08172
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#300705 Mental retardation, x-linked 17; mrx17 Q99714
%300852 Mental retardation, x-linked 88; mrx88 P50052
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613073 Metaphyseal anadysplasia 2; mandp2 P14780
#609634 Migraine, familial hemiplegic, 3; fhm3 P35498
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#126200 Multiple sclerosis, susceptibility to; ms P08575
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#159900 Myoclonic dystonia P14416
#202700 Neutropenia, severe congenital, 1, autosomal dominant; scn1 P08246
#601665 Obesity P32245
#164230 Obsessive-compulsive disorder; ocd P31645
#604715 Orthostatic intolerance P23975
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#167000 Ovarian cancer P04626
#613135 Parkinsonism-dystonia, infantile; pkdys Q01959
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#607276 Resting heart rate, variation in P08588
#275210 Restrictive dermopathy, lethal P02545
#607745 Seizures, benign familial infantile, 3; bfis3 Q99250
#608971 Severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-positive, nk cell-positive P08575
#609620 Short qt syndrome 1; sqt1 Q12809
#253300 Spinal muscular atrophy, type i; sma1 Q16637
#253550 Spinal muscular atrophy, type ii; sma2 Q16637
#253400 Spinal muscular atrophy, type iii; sma3 Q16637
#271150 Spinal muscular atrophy, type iv; sma4 Q16637
#190300 Tremor, hereditary essential, 1; etm1 P35462
#610379 West nile virus, susceptibility to P51681
#112100 Yt blood group antigen P22303

KEGG DISEASE (59)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
P35354 (related)
H00018 Gastric cancer P00533 (related)
P04626 (related)
H00022 Bladder cancer P00533 (related)
P04626 (related)
H00028 Choriocarcinoma P00533 (related)
P03956 (related)
P04626 (related)
H00030 Cervical cancer P00533 (related)
P04626 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00026 Endometrial Cancer P03372 (marker)
P04626 (related)
Q92731 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
H00019 Pancreatic cancer P04626 (related)
H00027 Ovarian cancer P04626 (related)
H00031 Breast cancer P04626 (related)
P04626 (marker)
H00046 Cholangiocarcinoma P04626 (related)
P35354 (related)
H00093 Combined immunodeficiencies (CIDs) P06239 (related)
H00079 Asthma P07550 (related)
H00100 Neutropenic disorders P08246 (related)
H00091 T-B+Severe combined immunodeficiencies (SCIDs) P08575 (related)
H00036 Osteosarcoma P08684 (marker)
H01205 Coumarin resistance P11712 (related)
H00025 Penile cancer P14780 (related)
P35354 (related)
H00479 Metaphyseal dysplasias P14780 (related)
H00548 Brunner syndrome P21397 (related)
H00769 Hyperekplexia P23415 (related)
H01031 Orthostatic intolerance (OI) P23975 (related)
H00490 Diaphyseal dysplasia with anemia (Ghosal) P24557 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00775 Familial or sporadic hemiplegic migraine P35498 (related)
H00783 Febrile seizures P35498 (related)
H00480 Non-syndromic X-linked mental retardation P50052 (related)
Q99714 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00720 Long QT syndrome Q12809 (related)
H00725 Short QT syndrome Q12809 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00606 Early infantile epileptic encephalopathy Q99250 (related)
H00806 Benign familial neonatal and infantile epilepsies Q99250 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

13 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D012640 Seizures C00001770
C00025213
D049188 Prenatal Injuries C00001770
C00025213
D009422 Nervous System Diseases C00001770
C00025213
D006930 Hyperalgesia C00001770
C00025213
D002375 Catalepsy C00001770
C00025213
D009374 Neoplasms, Experimental C00001695
D009101 Multiple Myeloma C00001695
D012206 Rhabdomyolysis C00001695
D008113 Liver Neoplasms C00001695
D002493 Central Nervous System Diseases C00001695
D002294 Carcinoma, Squamous Cell C00001695
D000741 Anemia, Aplastic C00001695
D058186 Acute Kidney Injury C00001695